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Visible‐Light‐Driven CO(2) Reduction by Mesoporous Carbon Nitride Modified with Polymeric Cobalt Phthalocyanine

The integration of molecular catalysts with low‐cost, solid light absorbers presents a promising strategy to construct catalysts for the generation of solar fuels. Here, we report a photocatalyst for CO(2) reduction that consists of a polymeric cobalt phthalocyanine catalyst (CoPPc) coupled with mes...

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Detalles Bibliográficos
Autores principales: Roy, Souvik, Reisner, Erwin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6771752/
https://www.ncbi.nlm.nih.gov/pubmed/31273886
http://dx.doi.org/10.1002/anie.201907082
Descripción
Sumario:The integration of molecular catalysts with low‐cost, solid light absorbers presents a promising strategy to construct catalysts for the generation of solar fuels. Here, we report a photocatalyst for CO(2) reduction that consists of a polymeric cobalt phthalocyanine catalyst (CoPPc) coupled with mesoporous carbon nitride (mpg‐CN(x)) as the photosensitizer. This precious‐metal‐free hybrid catalyst selectively converts CO(2) to CO in organic solvents under UV/Vis light (AM 1.5G, 100 mW cm(−2), λ>300 nm) with a cobalt‐based turnover number of 90 for CO after 60 h. Notably, the photocatalyst retains 60 % CO evolution activity under visible light irradiation (λ>400 nm) and displays moderate water tolerance. The in situ polymerization of the phthalocyanine allows control of catalyst loading and is key for achieving photocatalytic CO(2) conversion.